Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g17790 | A05 | 10062522 | G | A | upstream_gene_variant | MODIFIER | c.-4837G>A| |
S180 |
2 | BAA05g17790 | A05 | 10062531 | C | T | upstream_gene_variant | MODIFIER | c.-4828C>T| |
S155 |
3 | BAA05g17790 | A05 | 10062820 | C | T | upstream_gene_variant | MODIFIER | c.-4539C>T| |
S44 |
4 | BAA05g17790 | A05 | 10062844 | C | T | upstream_gene_variant | MODIFIER | c.-4515C>T| |
S172 S217 |
5 | BAA05g17790 | A05 | 10063320 | C | T | upstream_gene_variant | MODIFIER | c.-4039C>T| |
S251 |
6 | BAA05g17790 | A05 | 10063593 | C | T | upstream_gene_variant | MODIFIER | c.-3766C>T| |
S73 S91 |
7 | BAA05g17790 | A05 | 10063828 | G | A | upstream_gene_variant | MODIFIER | c.-3531G>A| |
S67 |
8 | BAA05g17790 | A05 | 10067552 | G | A | missense_variant | MODERATE | c.194G>A|p.Ser65Asn |
S274 |
9 | BAA05g17790 | A05 | 10067686 | G | A | missense_variant | MODERATE | c.328G>A|p.Asp110Asn |
S219 S72 |
10 | BAA05g17790 | A05 | 10070258 | C | T | downstream_gene_variant | MODIFIER | c.*2531C>T| |
S256 |
11 | BAA05g17790 | A05 | 10070618 | C | T | downstream_gene_variant | MODIFIER | c.*2891C>T| |
S295 |
12 | BAA05g17790 | A05 | 10070825 | G | A | downstream_gene_variant | MODIFIER | c.*3098G>A| |
S308 |